A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3612821



Internal ID12149047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88955213..88955802hg38UCSC Ensembl
chr16:89021621..89022210hg19UCSC Ensembl
chr16:87549122..87549711hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38590
hg19590
hg18590
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1211270
Supporting Variants
SamplesHuRef
Known GenesCBFA2T3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3612821
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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